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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 379389Generated: October 31, 2026

Hydrochloric Acid → Methyl-(6-morpholin-4-yl-4-o-tolyl-pyridin-3-yl)-amine

https://huagongshe.com/reaction/379389

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTrimethyl orthoformateHCID 9005—
ReactantSodium HydroxideHCID 14798—
Reactant6-Morpholin-4-yl-4-o-tolyl-pyridin-3-ylamineHCID 15486051—
ReactantAluminium lithium hydrideHCID 21226445—
CatalystTrifluoroacetic acidHCID 6422—
SolventTetrahydrofuranHCID 8028—
ProductMethyl-(6-morpholin-4-yl-4-o-tolyl-pyridin-3-yl)-amineHCID 1143755766%

Reaction Steps

A solution of 2.24 g (8.3 mmol) 6-morpholin-4-yl-4-o-tolyl-pyridin-3-ylamine in 17 ml trimethyl orthoformate and 3 drops trifluoroacetic acid was heated for 2 h at 130° C. The reaction mixture was evaporated and dried in vacuo for 30 min. The residual oil was dissolved in 5 ml tetrahydrofuran and was added dropwise under ice cooling to 630 mg (16.6 mmol) lithium aluminum hydride in 20 ml tetrahydrofuran. The reaction mixture was stirred for lh at room temperature, cooled to 0° C. again and acidified (pH 1-2) by addition of 28% hydrochloric acid solution. After stirring for 5 min, 28% sodium hydroxide solution was added to reach pH 10. The solution was filtered over celite, evaporated and purified by flash chromatography to give 1.56 g (66%) of the title compound as a white foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06297375B1
Source datasetuspto-grants-2001_10
ORD IDord-7a8906d067c44bc29e6183e9e9bf4616
Source noteuspto-grants-2001_10